Canonical Allele Identifier: CA343473033

Gene: RXRG

Linked Data

• dbSNP Id: rs1311764560
• gnomAD v3: 1-165419984-C-T
• gnomAD v4: 1-165419984-C-T
• MyVariant Identifiers: chr1:g.165389221C>T (hg19) ; chr1:g.165419984C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419984C>T , CM000663.2:g.165419984C>T	GRCh38
NC_000001.10:g.165389221C>T , CM000663.1:g.165389221C>T	GRCh37
NC_000001.9:g.163655845C>T	NCBI36
NG_029517.1:g.30372G>A
NG_029517.2:g.30372G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.328G>A MANE Select	ENSP00000352900.5:p.Glu110Lys
ENST00000359842.9:c.328G>A	ENSP00000352900.5:p.Glu110Lys
ENST00000470566.1:n.253G>A
ENST00000619224.1:c.-42G>A	ENSP00000482458.1:n.-42G>A
NM_001256570.1:c.-42G>A	NP_001243499.1:n.-42G>A
NM_001256571.1:c.-42G>A	NP_001243500.1:n.-42G>A
NM_006917.4:c.328G>A	NP_008848.1:p.Glu110Lys
NM_006917.5:c.328G>A MANE Select	NP_008848.1:p.Glu110Lys
NM_001256571.2:c.-42G>A	NP_001243500.1:n.-42G>A
NM_001256570.2:c.-42G>A	NP_001243499.1:n.-42G>A